A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859146



Internal ID22634081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133197423..133205950hg38UCSC Ensembl
chr9:136072810..136081337hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg388528
hg198528
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2211n209
Supporting Variantsnssv17511654
Samples
Known GenesOBP2B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859146
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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